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Research Article Free access | 10.1172/JCI118034

Identification of thyroid stimulating hormone receptor-specific T cells in Graves' disease thyroid using autoantigen-transfected Epstein-Barr virus-transformed B cell lines.

R J Mullins, S B Cohen, L M Webb, Y Chernajovsky, C M Dayan, M Londei, and M Feldmann

Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, United Kingdom.

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Published July 1, 1995 - More info

Published in Volume 96, Issue 1 on July 1, 1995
J Clin Invest. 1995;96(1):30–37. https://doi.org/10.1172/JCI118034.
© 1995 The American Society for Clinical Investigation
Published July 1, 1995 - Version history
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Abstract

The importance of thyrotropin receptor (TSHR) agonist antibodies in the manifestations of Graves' disease (GD) is recognized. There are, however, no convincing reports of TSHR-specific T cells. We have previously cloned T cells specific for thyroglobulin and thyroid peroxidase (TPO) from GD lymphoid infiltrates and used autologous EBV-transformed B cell lines (EBVL) transfected with an expression vector encoding TPO to efficiently detect TPO-specific T cells. Here we used EBVL transfected with TSHR to seek TSHR-specific T cells in the GD infiltrates, after cloning the in vivo activated T cells without antigen. 3 out of 30 clones responded vigorously and reproducibly to EBVL-TSHR, with a mean stimulation index > 7. Their release of IL-2, IL-4, and IL-10 after stimulation with soluble anti-CD3 and phorbol ester was indistinguishable from the other clones from this thyroid. However, they produced relatively little IFN gamma (median IL-4/IFN gamma ratio of 0.80) compared with the other clones (median IL-4/IFN gamma ratio 0.06). Thus, this new potent method of antigen presentation, using autoantigen-transfected EBVL, has permitted the first unequivocal identification of TSHR T cells in GD thyroid, with distinct Th0/Th2 characteristics, unlike previously cloned TPO-responsive cells which have Th1 characteristics.

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